Global Medical Device Podcast powered by Greenlight Guru

416 Épisodes

1. Bridging the Gap between Medical Devices and Clinical Data

   Publié: 20/04/2022
2. Navigating the Medical Device Single Audit Program (MDSAP)

   Publié: 13/04/2022
3. Bringing Augmented Reality MedTech to Market

   Publié: 07/04/2022
4. Making Your Informational Meetings with FDA Valuable & Worthwhile

   Publié: 30/03/2022
5. Building Your Bill of Materials (BOM) to Accommodate Crossfunctional Needs

   Publié: 23/03/2022
6. QMSR: The Future of FDA's Quality Management System Regulation for Medical Devices

   Publié: 16/03/2022
7. How Medical Device Intellectual Property Protection Varies by Sector

   Publié: 09/03/2022
8. Human Factors & Risk Management: What's Needed & Why?

   Publié: 02/03/2022
9. What are the Opportunities for Improvement (OFI) for Quality?

   Publié: 23/02/2022
10. Overcoming Barriers to Receiving 510(k) Clearance: One Company's Go-to-Market Triumph

    Publié: 17/02/2022
11. How to Select a Contract Manufacturer

    Publié: 02/02/2022
12. A Regulatory Gap Analysis of FDA's Systems & Policies

    Publié: 26/01/2022
13. Greenlight Guru Acquires CanvasGT: A Fire(less)side Chat

    Publié: 19/01/2022
14. Tips for Being Prepared Post-EUA (Emergency Use Authorization)

    Publié: 12/01/2022
15. Understanding the UDI System for Medical Devices

    Publié: 06/01/2022
16. Shaking Things Up: What's Next for the Global Medical Device Podcast

    Publié: 16/12/2021
17. How Augmented Reality (AR) is Revolutionizing Healthcare

    Publié: 09/12/2021
18. Why FDA is Prioritizing Clinical Decision Support Software & Why You Should Care

    Publié: 02/12/2021
19. Why Usability Matters

    Publié: 24/11/2021
20. A Special Glimpse into Medtronic's Recent Developments in Spine & Biologics Technology

    Publié: 17/11/2021